| Primary Device ID | B707128320000080 |
| NIH Device Record Key | 14dc60d3-fb22-42ca-b4a4-167f07c4f148 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KIT DUALX LLIF 10-13MM x 12 DEG x 50MM |
| Version Model Number | 12832000008 |
| Company DUNS | 081021000 |
| Company Name | Amplify Surgical, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |